Universal reference book for medicines
Name of the preparation: CAMPHOR UNGENTUM

Active substance: camphor

Type: Analgesic and topical anesthetic for external use

Manufacturer: TVERSKAYA PHARMACEUTICAL FACTORY (Russia)
Composition, form of production and packaging
?
Ointment for external use 100 g
camphor 10 g

Excipients: Vaseline 54 g, solid paraffin oil 8 g, lanolin anhydrous 28 g.

25 g - cans of orange glass (1) - packs of cardboard.

50 g - cans of orange glass (1) - packs of cardboard.

30 g - aluminum tubes (1) - cardboard packs.

40 g - aluminum tubes (1) - packs of cardboard.

INSTRUCTION FOR THE SPECIALIST.

Description of the drug approved by the manufacturer for the printed edition of 2011.

PHARMACHOLOGIC EFFECT

The drug of natural origin has antiseptic, local irritating, local, analgesic, and anti-inflammatory effects.
Exciting sensitive nerve endings of the skin, dilates the blood vessels and improves the trophism of organs and tissues.
PHARMACOKINETICS

When applied to the surface of the skin is partially absorbed, subjected to oxidation.
Oxidation products combine with glucuronic acid and are excreted by the kidneys. Part of camphor is excreted unchanged in the form of lungs and bile. Permeability through the BBB and placental barrier - high; secretion with mother's milk - high.
INDICATIONS

- myalgia;

- myositis;

- Arthralgia;

- sciatica;

- Prophylaxis of bedsore formation.

DOSING MODE

Outwardly.
A small amount of ointment is applied to the area of ​​pain and light movements are rubbed 2-3 times / day.
Prevention of decubitus formation: treatment of skin 2-3 times / day.
After applying the ointment, wash hands thoroughly. The course of treatment is 7-10 days.Conducting repeated courses of treatment is possible on the recommendation of a doctor.
SIDE EFFECT

Allergic skin reactions (urticaria), skin irritation, headache, dizziness.

CONTRAINDICATIONS

- violation of the integrity of the skin or inflammatory skin diseases at the site of the intended application (incl.

dermatitis, eczema);

- Pregnancy;

- lactation period;

- age under 18 years (due to lack of data);

- Hypersensitivity.

PREGNANCY AND LACTATION

Contraindicated in pregnancy and lactation.

APPLICATION FOR CHILDREN

Contraindicated in children under 18 years.

SPECIAL INSTRUCTIONS

Avoid getting the product on open wounds, eyes and mucous membranes.

Impact on the ability to drive vehicles and manage mechanisms

During the treatment period, care must be taken when driving vehicles and engaging in other potentially hazardous activities requiring increased concentration of attention and speed, psychomotor reactions



OVERDOSE

To date, no cases of overdose have been reported with the use of the drug.

DRUG INTERACTION

Not found.

TERMS OF RELEASE FROM PHARMACY

The drug is approved for use as a means of OTC.

TERMS AND CONDITIONS OF STORAGE

Store at a temperature of 12 ° to 15 ° C, in a place protected from light.

Shelf life - 4 years.

Do not use after the expiration date printed on the package.

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